Volume 14, Issue 5 (Sep-Oct 2020)                   mljgoums 2020, 14(5): 13-18 | Back to browse issues page


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Hakim Elahi A, Sharifi R, Mahmoodi M, Kassaee S M. Effect of Octopine on Oxidative Stress Indices and Serum Levels of Lipids and Trace Elements in Mice with Breast Cancer. mljgoums 2020; 14 (5) :13-18
URL: http://mlj.goums.ac.ir/article-1-1244-en.html
1- Hamedan Branch, Islamic Azad University, Hamedan, Iran.
2- Department of Biology, Faculty of Basic Sciences, Ahar Branch, Islamic Azad University, Ahar, Iran , rasoulsharifi.sci@gmail.com
Abstract:   (3008 Views)
Background and objectives: The aim of this study was to evaluate the effectiveness of octopine (phytogenic-derivative of arginine) on antioxidant indices, trace elements and lipid profiles of a mouse model of breast cancer.
Methods: In this study, 48 Balb/c mice were divided into six groups: healthy control, cancer control, cancer group receiving 50 mg of octopine, cancer group receiving 100 mg of octopine and cancer group receiving 150 mg of octopine. The octopine treatment was carried out for three weeks. The 4T1 cell line was used to induce cancer. Fasting blood samples were taken from mice to evaluate lipid profile, copper and zinc levels. Malondialdehyde, superoxide dismutase and glutathione peroxidase activity in breast tumor tissues was evaluated. Data were analyzed by SPSS 18 software using one-way ANOVA and t-test.
Results: Octopine had no significant effect on superoxide dismutase and glutathione peroxidase activity in the treatment group compared with the control cancer group. However, it significantly increased total antioxidant capacity and decreased malondialdehyde activities. Furthermore, treatment with octopine significantly decreased serum zinc, copper, TG, cholesterol and low-density lipoprotein levels but significantly increased high-density lipoprotein compared with the untreated cancer group.
Conclusion: Octopine administration is effective in reducing some oxidative stress indices and improving trace elements abnormalities and lipid profile in mouse models of breast cancer.
Full-Text [PDF 673 kb]   (673 Downloads)    
Research Article: Original Paper | Subject: Biochemistry
Received: 2019/08/27 | Accepted: 2020/03/7 | Published: 2020/08/24 | ePublished: 2020/08/24

References
1. Siegel LR, Miller D K, Jemal A. Cancer statistics. CA CANCER J CLIN. 2019; 69: 7-34. [DOI:10.3322/caac.21551]
2. Tauro M, McGuire J, Lynch CC. New approaches to selectively target cancer-associated matrix metalloproteinase activity. Cancer Metast. Rev. 2014; 33(4): 1043-1057. [DOI:10.1007/s10555-014-9530-4]
3. Gao CM, Takezaki T, Wu JZ, Liu YT, Ding JH, Li SP, et al. Poly-morphisms in thymidylate synthase and methylenetetrahydrofolate reductase genes and the susceptibility to esophageal and stomach cancer with smoking. Asian Pacific Journal of Cancer Prevention. 2004; 5(2): 133-8.
4. Abdel-Salam O, Youness E, Hafez H. The antioxidant status of the plasma in patients with breast cancer undergoing chemotherapy. Open Journal of Molecular and Integrative Physiology. 2011; 1: 29-35. DOI: 10.4236/ojmip.2011.13005. [DOI:10.4236/ojmip.2011.13005]
5. Rao S, Kumari S. Changes in plasma lipid peroxidation and the antioxidant system in women with breast cancer. International Journal of Basic and Applied Sciences. 2012; 1(4): 429-38. DOI: 10.14419/ijbas.v1i4.267. [DOI:10.14419/ijbas.v1i4.267]
6. Salganik RI, Solovyova NA, Dikalov SI, Grishaeva ON, Semenova LA, Popovsky AV. Inherited enhancement of hydroxyl radical generation and lipid peroxidation in the S strain rats results in DNA rearrangements, degenerative diseases, and premature aging. Biochem Biophys Res Commun. 1994; 199(2): 726-33.doi: 10.1006/bbrc.1994.1289. [DOI:10.1006/bbrc.1994.1289]
7. Yelinova V, Glazachev Y, Khramtsov V, Kudryashova L, Rykova V, Salganik R. Studies of human and rat blood under oxidative stress: changes in plasma thiol level, antioxidant enzyme activity, protein carbonyl content, and fluidity of erythrocyte membrane. Biochem Biophys Res Commun. 1996; 221(2): 300-3.doi: 10.1006/bbrc.1996.0590. [DOI:10.1006/bbrc.1996.0590]
8. Zhai H, Chen X, Hu Z. Study on the relationship between intake of trace elements and breast cancer mortality with chemometric methodsComputational Biology and Chemistry, 2003; 27(6): 581-86. doi: 10.1016/s1476-9271(03)00049-5. [DOI:10.1016/S1476-9271(03)00049-5]
9. MacDonald G, Nalvarte I, Smirnova T, Vecchi M, Aceto N, Doelemeyer A, et al. Memo is a copper-dependent redox protein with an essential role in migration and metastasis. Sci Signal. 2014; 7(329): ra56. [DOI:10.1126/scisignal.2004870]
10. Munir R, Usman H, Hasnain S, Smans K, Kalbacher H, Zaidi N. Atypical plasma lipid profile in cancer patients: Cause or consequence? Biochimie. 2014; 102: 9-18. doi: 10.1016/j.biochi.2014.03.010. [DOI:10.1016/j.biochi.2014.03.010]
11. Yoon JK, Frankel AE, Feun LG, Ekmekcioglu S, Kim KB. Arginine deprivation therapy for malignant melanoma. Clin Pharmacol. 2013; 5: 11-9. doi:10.2147/ CPAA.S37350.
12. Ekmekcioglu S, Ellerhorst JA, Prieto VG, Johnson MM, Broemeling LD, Grimm EA. Tumor iNOS predicts poor survival for stage III melanoma patients. Int J Cancer. 2006; 119: 861-6. [DOI:10.1002/ijc.21767]
13. Kim S-H, Roszik J, Grimm EA, Ekmekcioglu S. Impact of l-Arginine Metabolism on Immune Response and Anticancer Immunotherapy. Front Oncol. 2018, 8(67): 1-4 [DOI:10.3389/fonc.2018.00067]
14. Hockachka P, Hartline P, Fields J. Octopine as an end product of anaerobic glycolysis in the chambered nautilus. Science. 1997; 195(4273): 72-4. [DOI:10.1126/science.831256]
15. Smits SHJ, Mueller A, Schmitt L, Grieshaber MK. A Structural Basis for Substrate Selectivity and Stereoselectivity in Octopine Dehydrogenase from Pecten maximus. Journal of Molecular Biology. 2008; 381(1): 200-11. [DOI:10.1016/j.jmb.2008.06.003]
16. Soleimani N, Farhangi B, ashraf Mohabati mobarez, Fatemeh Etyabi. VEGF and MMP-9 Gene Expression Caused by Treatment with Helicobacter Pylori Neutrophilactivating Recombinant Protein in a Breast Cancer Model. JBUMS. 2015, 17(3): 13-19. [Persian]
17. Andrés A, Morales JM, Praga M, Campo C, Lahe17ra V, García-Robles R, et al. L-arginine reverses the antinatriuretic effect of cyclosporin in renal transplant patients. Nephrol Dial Transplant. 1997; 12(7): 1437-40. doi: 10.1093/ndt/12.7.1437. [DOI:10.1093/ndt/12.7.1437]
18. Jones LW, Viglianti BL, Tashjian JA, Kothadia SM, Keir ST, Freedland SJ, et al. Effect of aerobic exercise on tumor physiology in an animal model of human breast cancer. J Appl Physiol. 108(2): 343-8.doi:10.1152/japplphysiol.00424.2009. [DOI:10.1152/japplphysiol.00424.2009]
19. Benzie IF, Strain J. Ferric reducing/antioxidant power assay: Direct measure of total antioxidant activity of biological fluids and modified version for simultaneous measurement of total antioxidant power and ascorbic acid concentration. Methods in enzymology. 1999; 299: 15-27. [DOI:10.1016/S0076-6879(99)99005-5]
20. L'Abbé MR, Fischer PW. Automated assay of superoxide dismutase in blood. Methods in enzymology. 1990; 186: 232-7.doi: 10.1016/0076-6879(90)86113-a. [DOI:10.1016/0076-6879(90)86113-A]
21. Paglia DE, Valentine WN. Studies on the quantitative and qualitative characterization of erythrocyte glutathione peroxidase. J Lab Clin Med. 1967; 70(1): 158-169.
22. Sabarimuthu D, Pamakanthan SR. Effects of Epicatechin, a Flavonoid on Lipid Peroxidation and Antioxidant in STZInduced Diabetic Rats Liver, Kidney and Heart. Pharmacol Rep. 2005; 57(5): 610-615.
23. Burtis CA, Ashwood ER, Bruns DE. Tietz textbook of clinical chemistry and molecular diagnostics. 5th ed. USA: Elsevier. 2012; 1033-47.
24. Reedy BS, Charles MJ, Rajug NJ, Reddy S, Reddy S, Rama Lakshmi PVB, et al. Trace Elemental Analysis of Cancer - Afflicted Intestine by PIXE Technique. Biol Trace Elem Res. 2004; 102(1-3): 265-82. doi: 10.1385/bter:102:1-3:265. [DOI:10.1385/BTER:102:1-3:265]
25. O'Connor JM. Trace elements and DNA damage. Biochem Soc Trans. 2001; 29(Pt 2): 354-7. [DOI:10.1042/bst0290354]
26. Leccia MT, Richard MJ, Favier A, Beani JC. Zinc protects against ultraviolet A1-induced DNA damage and apoptosis in cultured human fibroblasts. Biol Trace ElemRes. 1999; 69(3): 177-190. DOI: 10.1007/BF02783870. [DOI:10.1007/BF02783870]
27. Adzersen KH, Jess P, Freivogel KW, Gerhard I, Bastert G. Raw and cooked vegetables, fruits, selected micronutrients, and breast cancer risk: a case-control study in Germany. Nutr Cancer. 2003; 46(2): 131-137. doi: 10.1207/S15327914NC4602_05. [DOI:10.1207/S15327914NC4602_05]
28. Skrajnowska D, Bobrowska B, Tokarz A, Kuras M, Rybicki P, Wachowicz M. The Effect of Zinc- and Copper Sulphate Supplementation on Tumor and Hair Concentrations of Trace Elements (Zn, Cu, Fe, Ca, Mg, P) in Rats with DMBA-Induced Breast Cancer. Pol J Environ Stud. 2011; 20(6):1585-1592.
29. Koksoy C, Kavas GO, Akcil E, Kocaturk PA, Kara S, Ozarslan C. Trace elements and superoxide dismutase in benign and malignant breast diseases. Breast Cancer Res Treat. 1997; 45(1): 1-6.
30. Valko M, Rhodes CJ, Moncol J, Izakovic M, Mazur M. Free radicals, metals and antioxidants in oxidative stress-induced cancer. Chem Biol Interact. 2006; 160(1):1-40. [DOI:10.1016/j.cbi.2005.12.009]
31. Jabecka A, Ast J, Bogdaski P, Drozdowski M, Pawlak-Lemaska K, Cielewicz AR, et al. Oral L-arginine supplementation in patients with mild arterial hypertension and its effect on plasma level of asymmetric dimethylarginine, L-citruline, L-arginine and antioxidant status. Eur Rev Med Pharmacol Sci. 2012; 16(12): 1665-74.
32. Lucotti P, Setola E, Monti LD, Galluccio E, Costa S, Sandoli EP, et al. Beneficial effects of a long-term oral L-arginine treatment added to a hypocaloric diet and exercise training program in obese, insulin-resistant type 2 diabetic patients. Am J Physiol Endocrinol Metab 2006; 291(5): E906-12. [DOI:10.1152/ajpendo.00002.2006]
33. Kochar N I, Umathe S. Beneficial effects of L-arginine against diabetes-induced oxidative stress in gastrointestinal tissues in rats. Pharmacological Reports; 2009, 16(4): 665-672. [DOI:10.1016/S1734-1140(09)70118-5]
34. Sharma M, Tuaine J, McLaren B, et al. Chemotherapy agents Alter plasma lipids in breast Cancer patients and show differential effects on lipid metabolism genes in liver cells. PLoS One. 2016; 11(1): e0148049. doi: 10.1371/journal.pone.0148049. [DOI:10.1371/journal.pone.0148049]
35. Alexopoulos CG, Blatsios B, Avgerinos A. Serum lipids and lipoprotein disorders in cancer patients. Cancer. 1987; 60(12): 3065-3070. https://doi.org/10.1002/1097-0142(19871215)60:12<3065::AID-CNCR2820601234>3.0.CO;2-Q [DOI:10.1002/1097-0142(19871215)60:123.0.CO;2-Q]
36. Borrelli R, del Sordo G, De Filippo E, Contaldo F, Parisi V, Beneduce G. High serum HDLcholesterol in pre- and post-menopausal women with breast cancer in southern Italy. Adv Exp Med Biol 1993; 348: 149-153. doi: 10.1007/978-1-4615-2942-2_17. [DOI:10.1007/978-1-4615-2942-2_17]
37. Knapp ML, Al-Sheibani S, Riches PG. Alterations of serum lipids in breast cancer: Effects of disease activity, treatment and hormonal factors. Clin Chem 1991; 37(12): 2093-2101. [DOI:10.1093/clinchem/37.12.2093]
38. Adana A, Llanos P, Makambi KH, Tucker CA. Cholesterol, lipoproteins, and breast cancer risk in African-American women. Ethn Dis. 2012; 22(3): 281-7.
39. Sato M, Nakano T, Takeuchi M, Kanno N, Nagahisa E, Sato Y, Kobatake Y. Effects of octopine on the serum cholesterol level in rats. Bioscience, Biotechnology and Biochemistry. 1996, 60(1): 154-156. DOI: 10.1271/bbb.60.154. [DOI:10.1271/bbb.60.154]

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This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.